Ramallo Marketing & Communications Job Listings

Occupational Health and Safety Manager64142407585923120

Indeed

Occupational Health and Safety Manager

Antares Technologies is looking for a person to fill the position of Occupational Health and Safety Manager to join our team in Villa Constitución, who will be responsible for ensuring compliance with current regulations regarding hygiene, safety, and occupational health, promoting a preventive culture, guaranteeing safe working conditions, and coordinating all actions related to the protection of people and organizational assets. **Main Responsibilities:** Develop and maintain up-to-date area documentation (policies, procedures, risk matrices, permits, and records), ensuring proper upload to customer portals and physical/digital archiving. Plan and deliver training in safety, occupational health, and environmental topics, ensuring traceability and content updates. Manage the distribution, control, and traceability of Personal Protective Equipment (PPE), including user and maintenance manuals. **Manage ART relationships:** submit required documentation, monitor accidents, conduct investigations, and implement corrective action plans. Coordinate pre-employment and periodic medical exams, tracking expiration dates and medical fitness records. Ensure compliance with legal requirements, ISO standards (9001 and 14001\), and specific industrial client demands. Participate in internal and external audits, proposing improvements and conducting regular plant visits. Promote a preventive culture through communication campaigns, advising leaders, and participating in safety committees. At Antares Technologies, we design and implement intelligent solutions that connect technology with production. We work with leading industries worldwide, delivering innovation, agility, and skilled human talent. We are a globally present company dedicated to providing Automation, IT, Robotics, Special Projects, and specialized Technical Staffing solutions. We offer consulting services, industrial software development, technical support, and related services. With offices in Argentina, Brazil, Mexico, and the USA, we respond to the needs of a growing market, providing comprehensive advisory services to our clients—from basic project guidelines to effective implementation. We have professional resources to fully manage the development process, with a flexible structure that allows us to adapt our services according to project requirements, consistently delivering distinctive and original solutions that create competitive advantages. Requirements Bachelor's degree in Occupational Hygiene and Safety. At least 4 years of prior experience in similar roles within industrial environments, both office and plant settings. Professional registration in the province of Buenos Aires; desirable registration in CABA and Santa Fe. Residency in San Nicolás or Villa Constitución. Full-time availability. Knowledge of labor legislation and occupational safety and hygiene regulations. Valid driver's license. Strong communication, planning, teamwork, and continuous improvement orientation. **Additional Skills:** Familiarity with ISO standards, Office suite, customer portals, and document management systems. Benefits Family healthcare insurance, ‍ work clothing. Employee referral program, personal loan policy, performance bonus, ongoing training (programs and platforms), and much more.

Av. Alberdi 361, B2900 San Nicolás de Los Arroyos, Provincia de Buenos Aires, Argentina

Indeed

Finance Specialist

### **Summary** The SSO Finance Specialist is accountable for budget planning, analytics and payment execution in a direct country or extended country group (OPC and satellite countries) in close collaboration with SSO Study Start\-Up Managers, SSO Clinical Project Managers and SSO Contracting Specialists in compliance with Novartis processes, GCP/ICH and regulatory requirements ### **About the Role** **Key responsibilities:** * Supports country SSU strategy in close collaboration with SSO Study Start\-Up Team Lead and SSO Study Start\-Up Managers to ensure SSU timelines and deliverables are met according to country commitments * Responsible for accounting and execution of investigator payments in a direct country or extended study group (OPC and satellite countries) in close collaboration with SSO Study Start\-Up Manager, SSO Clinical Project Manager and SSO Contracting Specialist in assigned projects * Project controlling \& budget management supports financial planning, forecasting and management, analyses and reports project costs and their drivers * Set up \& validation of investigator contracts in the accounting system for clinical studies * Executes and monitors internal controls * Translates Grant Plans into local Payment Schemes **Essential Requirements:** * Bachelor's degree in scientific, finance or economics discipline * Fluent in both written and speaking english and spanish languages. * Financial and business economics background * Independent, dynamic, structured and committed way of working * Communicates effectively in a local/global matrixed environment **Why Novartis:** Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people\-and\-culture **Join our Novartis Network:** Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network **Benefits and Rewards:** Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits\-rewards Division Development Business Unit Innovative Medicines Location Argentina Site Ramallo (Argentina) Company / Legal Entity AR01 (FCRS \= AR001\) Novartis Argentina S.A. Functional Area Research \& Development Job Type Full time Employment Type Regular Shift Work No

GXCH+HM Ramallo, Buenos Aires Province, Argentina

Patient Safety Specialist64142379743107122

Indeed

Patient Safety Specialist

### **Summary** Monitors and audits the company's surveillance program for drugs, biologics, or medical devices, including the intake, assessment, processing, and follow-up of adverse reports. Participates in addressing any legal liability and compliance with government regulations. Ensures accurate receipt, maintenance, and evaluation according to product labeling. Reports events or reactions as required by regulatory authorities, including adverse event data from clinical trials, spontaneous or solicited sources, periodic and experience reports. May enable trend and safety signal detection and assessment. Supports all clinical trial activities and post-marketing activities. ### **About the Role** Major Accountabilities \~ Supporting management of operational processes to ensure compliance with Novartis global/local procedures, national and international regulations/standards/guidelines for pharmacovigilance of marketed and investigational products from Novartis \~ Managing the collection, processing, documentation, reporting, and follow-up of all adverse event (AE) reports for all Novartis products from clinical trials, post-marketing studies (PMS), patient support programs (POP), registries, and all spontaneous reports (SR). \~ Accurately and consistently transcribe, translate (if necessary), and enter data from all serious adverse events (from clinical trials) and all adverse events (from POPs, PMS, registries, and all SRs) into safety systems from source documents, emphasizing timeliness and quality. \~ Recording and tracking evidence, submissions, and distribution of documents such as SAEs, SRs, investigator notifications, etc., in collaboration with other departments \~ Managing the reporting/submission/distribution of safety reports/updates/information to local health authorities and/or clinical operations in coordination with other departments. \~ Collaborating with other local/global PV staff to ensure accurate evaluation of safety data. \~ Interacting and exchanging relevant safety information with LHAs, PV staff, other functional groups, and third parties as appropriate. \~ Gathering and monitoring global/regional/national (where applicable) pharmacovigilance regulations and providing updates to the global PVO organization. \~ Developing, updating, and implementing local procedures to ensure compliance with global PVO procedures and national requirements. \~ Managing and maintaining all relevant assigned PVO databases, where applicable. \~ Developing and updating pharmacovigilance training materials \~ Ensuring support and de-escalation of audits, corrective actions and preventive actions (CAPA), and health authority inspections. \~ Providing timely, relevant information to study coordinators, rating agencies, and other Novartis employees \~ Distribution of marketing samples (if applicable) Key Performance Indicators Monitors and audits the company's surveillance program for drugs, biologics, or medical devices, including the intake, assessment, processing, and follow-up of adverse reports. Participates in addressing any legal liability and compliance with government regulations. Ensures accurate receipt, maintenance, and evaluation according to product labeling. Reports events or reactions as required by regulatory authorities, including adverse event data from clinical trials, spontaneous or solicited sources, periodic and experience reports. May enable trend and safety signal detection and assessment. Supports all clinical trial activities and post-marketing activities. Work Experience \~Operations Management and execution \~Cross-border collaboration \~Functional breadth Skills \~Filing (documents) \~Pharmacovigilance \~Safety science insights \~Databases \~Employee training \~Reporting Language English **Why Novartis:** Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people\-and\-culture **Join our Novartis Network:** Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network **Benefits and Rewards:** Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits\-rewards Division Development Business Unit Innovative Medicines Location Argentina Site Ramallo (Argentina) Company / Legal Entity AR01 (FCRS \= AR001\) Novartis Argentina S.A. Functional Area Research \& Development Job Type Part time Employment Type Regular Shift Work No

GXCH+HM Ramallo, Buenos Aires Province, Argentina